Human Phenotype Ontology 
Grandparent Node:
Abnormal medial rectus muscle physiology (HP:0025606)help
Parent Node:
Medial rectus muscle weakness (HP:0031753)help
..Starting node
Medial rectus muscle restriction (HP:0031757)help
Term ID: 31757
Name: Medial rectus muscle restriction
Definition: Mechanical limitation of the range of movement of the medial rectus muscle.
Reference: HP:0031757
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandMedial rectus muscle underaction (HP:0031756) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031757HP:0031757Medial rectus muscle restriction0 CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.